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  • Nutraceuticals/Dietary Supplements: FDA Regulatory
    Submission and Manufacturing Quality Requirements

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Thursday - Jun 27, 2013 10:00 AM
  • End Time:
  • Thursday - Jun 27, 2013 11:00 AM
  • Location:
  • Online
  • This dietary supplements quality compliance training will review the FDA regulatory requirements for manufacturing and commercialization of dietary supplements. You will gain a complete understanding of FDA requirements for manufacturing of nutraceuticals, food drugs, and dietary supplements.

    Why Should You Attend:

    Do you have responsibility the manufacturing or distribution of a dietary supplement, nutraceutical, or food drug? Are you considering launching a product into this rapidly growing market? Do you provide contract manufacturing capabilities for pharmaceuticals and want to learn more about dietary supplement GMP requirements?

    If yes, you should consider attending this one-hour webinar which will educate you on the regulatory and quality compliance requirements for these products.

    This session will review FDA regulatory requirements, review 21CFR part 111 covering dietary supplements, analyze applicable regulatory guidance documents, and highlight the increasing warning letter trend from FDA for dietary supplement manufacturers.

    Learning Objective:

    At the end of this webinar, participants will understand regulatory and quality compliance requirements for dietary supplements (often called food drugs, nutraceuticals, etc.)

    Areas Covered in The Webinar:

    - Review of FDA regulations in this area.
    - History of Dietary Supplement Health and Education Act.
    - Review 21CFR part 111 requirements.
    - Review applicable FDA guidance documents.
    - Overview the key elements of the quality system dietary supplement companies should implement to be GMP compliant.
    - Analysis of Warning Letter trends among dietary supplement manufacturers.
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